Contract Manufacturing for the Life Science Industry
We offer leading expertise in manufacturing biomedical devices for the growing life science and biotech sectors.
Experience in the Lifescience Industry
The future of medicine is in innovation with developments in life sciences and biotechnology devices at the cutting edge. We’re proud to offer our medical device development services for the biotech industry to help our clients develop medical device advances, conduct research, and make breakthroughs.
Innovation and integrity are central to any project we work on, be it a complete device or an individual part. Our complete development process brings all the steps under one roof to reduce time delays and streamline the process from start to finish.
As an expert medical device developer with over 40 years of experience, we are committed to creating components to exacting standards for this industry and helping drive the innovation inherent in the UK’s biotechnology industry. Call us today to find out more about our team’s broad range of experience, and how this places us perfectly to support your biotech and life science projects.
Bringing your BioTech Device to Market
Europlaz is a key player in the lifesciences and biotech industries by providing engineering, validation, prototyping, pilot production, design for manufacturing (DFM), design for assembly (DFA), contract manufacturing, regulatory approval and logistics services.
Biotechnology devices are essential for advancing research, drug development, diagnostics, and the production of biotechnological products. They enable scientists and biotechnologists to manipulate and study biological systems, leading to breakthroughs in fields like genomics, proteomics, personalised medicine, and bioprocessing.
Europlaz provides a wide range of services to life science companies, offering expertise, facilities, and capabilities that may not be available in-house. Contract manufacturing is common in the life science industry for various reasons, including cost-effectiveness, expertise, and scalability. We deliver fully compliant, market ready products for the lifescience industry.
Types of BioTech Devices
Europlaz has experience of manufacturing highly bespoke biomedical consumables within cleanrooms, with units ranging from thousands to hundreds of thousands per production run.
Much of our work in the BioTech market falls under confidentially agreements.
However, opposite are some common categories of BioTech devices that we can help manufacture components and parts for. Scroll through the images for a complete list.
To find out more please contact us today.
How Europlaz can Help
Bringing a biotech device to market requires careful planning, adherence to strict regulatory standards, and a thorough understanding of the needs of healthcare professionals and patients. That’s why it’s advisable to seek expert advice, especially in the areas of regulatory affairs, clinical trials, and quality management systems, to navigate the complex landscape of bringing a biotech device to market successfully.
Europlaz work alongside biomedical design agencies and leading biotech companies to design and manufacture uniquely powerful and cost-effective biomaterial innovations of the highest quality.
From an understanding of current technologies to working with new designs and materials, we offer a complete device design and development plan including prototyping, production, and testing. This is completed in our state-of-the-art facility with cleanroom capabilities.
Book a Meeting
To learn more about Europlaz’s services and the different medical devices we have helped develop, book a telephone meeting with one of the team.
To do this simply use the Schedule Meeting button below.
Since 1970 we have built a reputation for innovation, quality, and cost-effectiveness.
We use our experience and state-of-the-art technology to streamline all stages of the medical device manufacturing process for you – moving your product quickly and safely through development, and speeding up regulatory approval of medical devices.
Our UK-based ISO 13485 certified and FDA-compliant facility means that we have complete control of the process, from under one roof. We are flexible, and resourceful, and can take on projects of any size. Our clients range from small start-ups to international blue chip medical device suppliers.